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Term:
night blindness
(DOID:8499)
Annotations:
Rat: (31)
Mouse: (29)
Human: (30)
Chinchilla: (27)
Bonobo: (27)
Dog: (29)
Squirrel: (28)
Pig: (27)
Parent Terms
Term With Siblings
Child Terms
retinal disease
+
Vision Disorders
+
Al Gazali Sabrinathan Nair Syndrome
Alice in Wonderland Syndrome
amblyopia
+
angioid streaks
+
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction
Ausems Wittebol-Post Hennekam Syndrome
bestrophinopathy
Bietti crystalline corneoretinal dystrophy
blindness
+
Bothnia retinal dystrophy
bradyopsia
Central Serous Chorioretinopathy
Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation
Cerebral Visual Impairment and Intellectual Disability
chorioretinal scar
+
cone dystrophy
+
Creutzfeldt-Jakob Disease, Heidenhain Variant
Diplopia
distal arthrogryposis type 5
enhanced S-cone syndrome
familial benign fleck retina
FLOTCH Syndrome
fundus albipunctatus
Grouped Pigmentation of the Macula
Hemianopsia
hypertensive retinopathy
Iris Hypoplasia and Glaucoma
Leber congenital amaurosis
+
Low Vision
Microcephaly and Chorioretinopathy
+
Microcephaly with Chorioretinopathy, Autosomal Dominant
neovascular inflammatory vitreoretinopathy
nerve fibre bundle defect
night blindness
+
A retinal disease that is characterized by difficulty or the inability to see in relatively low light. (DO)
Photophobia
+
Rambaud Galian Syndrome
Ramos Arroyo Clark Syndrome
Retina Reperfusion Injury
Retinal Aplasia
retinal arterial tortuosity
retinal artery occlusion
+
retinal degeneration
+
retinal detachment
+
Retinal Dysplasia
+
retinal dystrophy with leukodystrophy
retinal edema
+
Retinal Hemorrhage
+
Retinal Neoplasms
+
Retinal Neovascularization
retinal perforation
+
retinal vascular disease
+
retinal vasculopathy with cerebral leukodystrophy
retinitis
+
retinopathy of prematurity
+
Roifman Syndrome
rubeosis iridis
scotoma
+
Sickle Cell Retinopathy
Siegler Brewer Carey Syndrome
Spatial Visualization, Aptitude For
Susac Syndrome
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia
abnormal threshold of rods
dominant pericentral pigmentary retinopathy
Duchenne Muscular Dystrophy, Mental Retardation, and Absence of ERG B-wave
Fleck Retina of Kandori
hereditary night blindness
+
Night Blindness Skeletal Anomalies Unusual Facies
Synonyms
Exact Synonyms:
nyctalopia
Primary IDs:
MESH:D009755
Xrefs:
ICD10CM:H53.6
;
ICD9CM:368.6
;
NCI:C34850
;
NCI:C37997
Definition Sources:
https://en.wikipedia.org/wiki/Nyctalopia
"DO" "DO"